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Drugs for Parkinson's Disease
The Medical Letter on Drugs and Therapeutics • Feb 22, 2021 (Issue 1618)
are thought to be caused by degeneration of
other neurotransmitter systems.1,2 No disease-modifying
drugs ...
The motor symptoms of Parkinson's disease (PD) are
caused primarily by degeneration of dopaminergic
neurons in the substantia nigra. The nonmotor symptoms
of the disease are thought to be caused by degeneration of
other neurotransmitter systems. No disease-modifying
drugs are available for treatment of PD.
Budesonide/Formoterol (Symbicort) for Asthma
The Medical Letter on Drugs and Therapeutics • Feb 11, 2008 (Issue 1279)
.
1,2
CLINICAL STUDIES — In a randomized, doubleblind trial in 596 patients >12 years old with moderate ...
A combination of the corticosteroid budesonide and the long-acting beta2-agonist formoterol (Symbicort - AstraZeneca) has become available in a metered dose inhaler for long-term maintenance treatment of asthma in patients ≥ 12 years old. A combination product that contains fluticasone propionate and salmeterol (Advair) is already available for this indication in the US. Neither one of these combinations is approved for acute treatment of asthma symptoms. A dry powder inhaler formulation of Symbicort has been available in Europe and Canada for several years.
Vanzacaftor, Tezacaftor, and Deutivacaftor (Alyftrek) for Cystic Fibrosis
The Medical Letter on Drugs and Therapeutics • Mar 17, 2025 (Issue 1724)
of elexacaftor, tezacaftor, and
ivacaftor, is FDA-approved for the same indication in
patients ≥2 years old.1 ...
The FDA has approved Alyftrek (Vertex), an oral
fixed-dose combination of the cystic fibrosis
transmembrane conductance regulator (CFTR)
modulators vanzacaftor, tezacaftor, and deutivacaftor,
for once-daily treatment of cystic fibrosis (CF) in
patients ≥6 years old who have at least one F508del
mutation or another responsive mutation in the
CFTR gene. This is the first approval for vanzacaftor
and for deutivacaftor, a deuterated form of ivacaftor.
Trikafta, a twice-daily oral fixed-dose combination of
elexacaftor, tezacaftor, and ivacaftor, is FDA-approved
for the same indication...
Med Lett Drugs Ther. 2025 Mar 17;67(1724):41-3 doi:10.58347/tml.2025.1724a | Show Introduction Hide Introduction
Delayed-Release Prednisone (Rayos)
The Medical Letter on Drugs and Therapeutics • Nov 26, 2012 (Issue 1404)
be
helpful in relieving these symptoms.1,2
CLINICAL STUDIES — A 12-week double-blind trial in
350 patients ...
The FDA has approved a delayed-release oral formulation
of prednisone (Rayos – Horizon Pharma). Rayos is
not labeled for any specific indication, but the only
published studies of the new product have been in
patients with rheumatoid arthritis (RA).
Laser Treatment of Onychomycosis
The Medical Letter on Drugs and Therapeutics • Feb 18, 2013 (Issue 1410)
of the fingernails or toenails can persist
for months or years despite topical and systemic
antimicrobial therapy.1 ...
Fungal infections of the fingernails or toenails can persist
for months or years despite topical and systemic
antimicrobial therapy. The FDA has cleared several
short-pulse laser systems for treatment of this mainly
cosmetic disorder.
Low-Dose Aspirin for Prevention of Preeclampsia
The Medical Letter on Drugs and Therapeutics • Jun 23, 2014 (Issue 1445)
for preeclampsia take low-dose aspirin daily after
the first trimester.1,2
PREECLAMPSIA — Preeclampsia ...
The American College of Obstetricians and Gynecologists
(ACOG) and the US Preventive Services Task
Force (USPSTF) have recommended that women at
risk for preeclampsia take low-dose aspirin daily after
the first trimester.
In Brief: Doxycycline for STI Post-Exposure Prophylaxis
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
(MSM) and transgender women (TGW) who had a bacterial STI within the previous 12 months.1
CLINICAL ...
The CDC has issued a recommendation for use
of a single dose of doxycycline for post-exposure
prophylaxis (PEP) of bacterial sexually transmitted
infections (STIs), specifically syphilis, chlamydia, and
gonorrhea, in men who have sex with men (MSM) and
transgender women (TGW) who had a bacterial STI
within the previous 12 months.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):119-20 doi:10.58347/tml.2024.1707f | Show Introduction Hide Introduction
Intranasal Triamcinolone For Allergic Rhinitis
The Medical Letter on Drugs and Therapeutics • Dec 13, 1991 (Issue 859)
Inhalation Daily Adult Dosage Cost*
Beclomethasone
Beconase − Allen & Hanburys 42 µg 1 spray each nostril 2 ...
An intranasal formulation of the corticosteroid triamcinolone (Nasacort - Rh ne- Poulenc Rorer) was recently approved by the US Food and Drug Administration for once-daily treatment of seasonal and perennial allergic rhinitis.
Cabergoline for Hyperprolactinemia
The Medical Letter on Drugs and Therapeutics • Jun 20, 1997 (Issue 1003)
), the drug most commonly used
for this condition, is also a D
2
agonist, but affects D
1
receptors ...
Cabergoline (Dostinex - Pharmacia & Upjohn), an ergot alkaloid derivative recently marketed for treatment of hyperprolactinemia, is a selective D2 dopamine agonist that inhibits prolactin-secreting cells in the pituitary. Bromocriptine (Parlodel - Sandoz), the drug most commonly used for this condition, is also a D2 agonist, but affects D1 receptors as well.
A New Rabies Vaccine
The Medical Letter on Drugs and Therapeutics • Jun 19, 1998 (Issue 1029)
receive post-exposure prophylaxis every year (DL Noah et al, Ann Intern Med, 128:922, June 1,
1998 ...
RabAvert (Chiron), a new human rabies vaccine prepared in purified chick embryo cell culture (PCEC), has been marketed in the USA for pre- and post-exposure prophylaxis. It is available in other countries as Rabipur. Human rabies is rare in the United States, but thousands of people receive post-exposure prophylaxis every year (DL Noah et al, Ann Intern Med, 128:922, June 1, 1998).
